Ikya Global
Job Description:
Responsible for compiling, formatting, and submitting regulatory documents electronically to global health authorities.
Key Responsibilities:
- Prepare eCTD and NeeS submissions
- Manage document publishing timelines
- Ensure submission accuracy and compliance
- Coordinate with regulatory teams globally
- Maintain submission archives and tracking systems
- Support regulatory audits and inspections
Qualification:
B.Pharm / M.Pharm / Life Sciences
